The availability of whole genome sequences in public databases permits genome-wide comparative studies of various bacterial species. Whole genome sequence-single nucleotide poly-morphisms (WGS-SNP) analysis has been used in recent studies and allows the discrimination of various Brucella species and strains. In the present study, 13 Brucella spp. strains from cattle of various locations in provinces of South Africa were typed and discriminated. WGS-SNP analysis indicated a maximum pairwise distance ranging from 4 to 77 single nucleotide polymorphisms (SNPs) between the South African Brucella abortus virulent field strains. Moreover, it was shown that the South African B. abortus strains grouped closely to B. abortus strains from Mozambique and Zimbabwe, as well as other Eurasian countries, such as Portugal and India. WGS-SNP analysis of South African B. abortus strains demonstrated that the same genotype circulated in one farm (Farm 1), whereas another farm (Farm 2) in the same province had two different genotypes. This indicated that brucellosis in South Africa spreads within the herd on some farms, whereas the introduction of infected animals is the mode of transmission on other farms. Three B. abortus vaccine S19 strains isolated from tissue and aborted material were identical, even though they originated from different herds and regions of South Africa. This might be due to the incorrect vaccination of animals older than the recommended age of 4–8 months or might be a problem associated with vaccine production.

Whole genome sequence analysis of brucella abortus isolates from various regions of South Africa / Ledwaba M.B.; Glover B.A.; Matle I.; Profiti G.; Martelli P.L.; Casadio R.; Zilli K.; Janowicz A.; Marotta F.; Garofolo G.; van Heerden H.. - In: MICROORGANISMS. - ISSN 2076-2607. - ELETTRONICO. - 9:3(2021), pp. 570.1-570.14. [10.3390/microorganisms9030570]

Whole genome sequence analysis of brucella abortus isolates from various regions of South Africa

Ledwaba M. B.;Glover B. A.;Profiti G.;Martelli P. L.;Casadio R.;
2021

Abstract

The availability of whole genome sequences in public databases permits genome-wide comparative studies of various bacterial species. Whole genome sequence-single nucleotide poly-morphisms (WGS-SNP) analysis has been used in recent studies and allows the discrimination of various Brucella species and strains. In the present study, 13 Brucella spp. strains from cattle of various locations in provinces of South Africa were typed and discriminated. WGS-SNP analysis indicated a maximum pairwise distance ranging from 4 to 77 single nucleotide polymorphisms (SNPs) between the South African Brucella abortus virulent field strains. Moreover, it was shown that the South African B. abortus strains grouped closely to B. abortus strains from Mozambique and Zimbabwe, as well as other Eurasian countries, such as Portugal and India. WGS-SNP analysis of South African B. abortus strains demonstrated that the same genotype circulated in one farm (Farm 1), whereas another farm (Farm 2) in the same province had two different genotypes. This indicated that brucellosis in South Africa spreads within the herd on some farms, whereas the introduction of infected animals is the mode of transmission on other farms. Three B. abortus vaccine S19 strains isolated from tissue and aborted material were identical, even though they originated from different herds and regions of South Africa. This might be due to the incorrect vaccination of animals older than the recommended age of 4–8 months or might be a problem associated with vaccine production.
2021
Whole genome sequence analysis of brucella abortus isolates from various regions of South Africa / Ledwaba M.B.; Glover B.A.; Matle I.; Profiti G.; Martelli P.L.; Casadio R.; Zilli K.; Janowicz A.; Marotta F.; Garofolo G.; van Heerden H.. - In: MICROORGANISMS. - ISSN 2076-2607. - ELETTRONICO. - 9:3(2021), pp. 570.1-570.14. [10.3390/microorganisms9030570]
Ledwaba M.B.; Glover B.A.; Matle I.; Profiti G.; Martelli P.L.; Casadio R.; Zilli K.; Janowicz A.; Marotta F.; Garofolo G.; van Heerden H.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/870949
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